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Metallic surfaces and particles can interact with fluorescent species, and modify their properties. Here, we used Au NP films, coated with dielectric layers of tunable thicknesses, and topped with a monolayer of the fluorophore tris(bipyridine)ruthenium(II). We found multiple distance-dependent effects, with a long-range interaction, mediated by thin-film interference, as we explored in previous work. We found that the NP film can quench the emission for very close NP-fluorophore separations (~2 nm), but enhances its magnitude (by a factor of 4-5) for longer separations, up to hundreds on nanometers. This is a result of the NPs interacting and acting as a far-field mirror; individual NPs only interact with fluorophores up to a distance of a few tens of nanometers. The radiative lifetime of the fluorophore is shortened due to the interaction. We also observed an effect previously predicted in theory studies, but not shown experimentally - the emission wavelength and peak widths were modified by the interaction.

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This page is a summary of: Distance-dependent fluorescence of tris(bipyridine)ruthenium(ii) on supported plasmonic gold nanoparticle ensembles, Nanoscale, January 2014, Royal Society of Chemistry,
DOI: 10.1039/c4nr04237a.
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